Clinical Trials Directory

Trials / Terminated

TerminatedNCT00271245

Selenium Supplementation of Patients With Cirrhosis

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
99 (actual)
Sponsor
Vanderbilt University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether patients with liver cirrhosis can improve their selenium nutritional status by taking supplemental selenium.

Detailed description

Selenium is an essential nutrient. Selenium carries out its biological functions through selenoproteins. The liver converts dietary selenium to a form that can be used to make selenoproteins. Patients with cirrhosis have much lower selenium levels than healthy individuals. We hypothesize that patients with cirrhosis are unable to utilize dietary selenium for selenoprotein synthesis. These patients may benefit from another form of selenium: selenate. We will compare the effects of two supplemental forms of selenium on plasma selenium levels in patients with cirrhosis. Patients will be randomized to receive either a placebo, 200 µg selenomethionine, 200 µg selenate or 400 µg selenate, daily, for 8 weeks. We will measure selenium levels in the blood at baseline, week 4 and week 8. We will determine which forms of selenium, if any, increased plasma selenium levels of the cirrhosis patients.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENT200 µg selenium as selenate200 µg selenium as selenate
DIETARY_SUPPLEMENT400 µg selenium as selenate400 µg selenium as selenate
DIETARY_SUPPLEMENT200 µg selenium as selenomethionine200 µg selenium as selenomethionine
DIETARY_SUPPLEMENTPlaceboPlacebo

Timeline

Start date
2006-02-01
Primary completion
2012-03-01
Completion
2012-03-01
First posted
2005-12-30
Last updated
2012-03-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00271245. Inclusion in this directory is not an endorsement.